Clinical Research Specialist (Entry Level)

at  Teckro Limited

ABOUT TECKRO

We founded Teckro to simplify and modernize clinical trials. In fact, thousands of clinical trial investigators and research site staff rely on Teckro to make the most informed decisions for their patients.
That’s where you come in. We’re offering you a role with purpose. Your contribution at Teckro will lead to faster, safer and more efficient clinical trials. Quality of life will be improved. In the end, lives will be saved.
Could you be our newest Teckronaut?
Expectations include the ability to build relationships (internally and externally), identify client needs, deliver our strategic and innovative solutions, and ensure that client contracts are delivered on time and on budget. A program director is responsible for ensuring a superior client experience and driving account growth.
This experienced professional exhibits decision quality, action orientation, communication savvy, and resourcefulness to meet both Teckro and client needs.

QUALIFICATIONS REQUIRED:

• Degree in biological science, pharmacy, pharmacology, other health-related field or prior qualifications or experience in technical communications preferred
• Genuine interest in clinical research, medical advancement and drug and biotechnology development highly beneficial as there is room for advancement within the Clinical Trials area in Teckro.
• Excellent computer skills

TECKRO BENEFITS:

• 25 days holidays
• Pension
• Healthcare
• Life Insurance
• Share Options
• 50% Maternity leave pay after capped length of service
• Paid Paternity leave scheme
• Bike to Work/ Tax Saver Scheme
• Gym/Wellness Allowance
• Sports and Social Club
  We are always looking for amazing people to join our growing team. If you are curious, passionate and motivated, then we want to talk to you!
  By submitting your application, you agree that Teckro may collect your personal data for recruiting and related purposes. Teckro’s Recruitment Privacy Statement explains what personal information Teckro may process, where Teckro may process your personal information, its purposes for processing your personal information, and the rights you can exercise over Teckro’s use of your personal information.

• Analyse, understand, and process complex scientific/medical/pharmaceutical information
• Work with study teams and internal project teams to ensure timely delivery of high-quality solutions
• Execute the layout and structure of clinical information required to utilize our products efficiently and effectively
• Monitor, analyse, and action end user feedback and usage analysis metrics to evaluate and improve usability and accuracy of our products
• Undertake other duties in-line with your role expertise and business requirements as required